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Impact of Forced Diuresis on the Residual Fragment Rate After Flexible Ureteroscopy for Destruction of Kidney Stones With Laser (FIREStones)

Primary Purpose

Kidney Stone

Status
Not yet recruiting
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Furosemide 40 mg
Sponsored by
University Hospital, Tours
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Kidney Stone

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients ≥ 18 years old and < 80 years old With the need to perform a flexible ureteroscopy with destruction of the kidney stones with laser Participants covered by or entitled to social security Written informed consent obtained from the participant Ability for participant to comply with the requirements of the study Exclusion Criteria: Persons covered by articles L1121-5 to L1121-8 of the CSP (corresponding to all protected persons: pregnant women, parturients, nursing mothers, persons deprived of their liberty by judicial or administrative decision, minors, and persons subject to a legal protection measure: guardianship or trusteeship) Contra-indication to Furosemide: Hyper-sensitivity to the active substance or one of the excipients Hyper-sensitivity to Sulfonamide Renal failure with oligo-anuria refractory to Furosemide Hypokalemia < 3,5 mmol/L Severe hyponatremia Hypovolemia with or without hypotension or dehydration Ongoing hepatitis, hepatic insufficiency severe and hepatic encephalopathy Patient having Furosemide as usual treatment Patient requiring an injection of Aminoside or Vancomycin before or during the procedure Participation in other interventional research with an investigational drug or medical device

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Furosemide

    Usual care

    Arm Description

    Injection of 40 mg of Furosemide during 10 minutes after the end of the flexible ureteroscopy for destruction of kidney stones with laser.

    Usual care, without injection of Furosemide.

    Outcomes

    Primary Outcome Measures

    Rate of stone free patients
    Rate of stone-free patients 3 months after a flexible ureteroscopy for renal stone laser destruction, evaluated on the low dose abdomino-pelvic CT-Scan. A centralized review of the images will be performed by two specialized radiologists, in a blind and crossed way to allow a homogenization of the results

    Secondary Outcome Measures

    Rate of urinary infection
    Rate of post-operative urinary tract infection will be assessed within 30 days after surgery on the combination of: Fever higher than 38.5°C and/or, Chills and/or, Clinical symptoms (supra-pubic pain, dysuria, pollakiuria, urgency, urinary burning, back pain radiating to the genitals, hematuria) and/or Positive urine culture with a significant bacteriuria threshold defined as bacteriuria ≥10^5 UFC/mL with one or two bacterial species.
    Pain in a scale
    Post-operative pain will be assessed on numerical pain scale in the recovery room, in the service and at the discharge. Pain scale is from 0 (no pain) to 10 (as bad as it could be nothing else matters)
    Opioid consumption
    The use of opioids will be reported
    Number of participants with adverse events
    Number of participants with Furosemide adverse events

    Full Information

    First Posted
    June 14, 2023
    Last Updated
    October 2, 2023
    Sponsor
    University Hospital, Tours
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05916963
    Brief Title
    Impact of Forced Diuresis on the Residual Fragment Rate After Flexible Ureteroscopy for Destruction of Kidney Stones With Laser
    Acronym
    FIREStones
    Official Title
    FIRESTONES : Impact of Forced Diuresis on the Residual Fragment Rate After Flexible Ureteroscopy for Destruction of Kidney Stones With Laser: a Randomized Controlled Two-parallel Group Multicenter Trial With Blinding Evaluation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    October 15, 2023 (Anticipated)
    Primary Completion Date
    January 15, 2026 (Anticipated)
    Study Completion Date
    January 15, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University Hospital, Tours

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    In view of the positive results of the numerous studies conducted on forced diuresis after extra-corporeal lithotripsy, the investigators chose to evaluate forced diuresis by injection of Furosemide associated with intravenous hydration, which has never before been the subject of a specific analysis.
    Detailed Description
    Flexible ureteroscopy is the most common technique to treat kidney stones and is the treatment of choice in France. Kidney stones destruction requires its laser pulverization into small fragments in order to remove them through the ureter or improve their spontaneous expulsion along the urinary tract. However, most of the time, all the micro-fragments and dust created during stone destruction cannot be extracted using our surgical tools, and may stay intra-renally at the end of the procedure. Although these micro-fragments are expected to disappear spontaneously by the natural flushing and peristalsis of the upper urinary tract, they remain at risk of stagnation that could be the nest of new aggregation and stone formation. Adjuvant treatments (such as forced diuresis, inversion or mechanical pressure) were previously described to improve the expulsion of stone fragments after extra-corporeal shock wave lithotripsy. Nevertheless, the impact of adjuvant treatment after flexible ureteroscopy remains unclear and mainly theoretical. In view of the positive results of the numerous studies conducted on forced diuresis after extra-corporeal lithotripsy, the investigators chose to evaluate forced diuresis by injection of Furosemide associated with intravenous hydration, which has never before been the subject of a specific analysis. Loop diuretics (including Furosemide) significantly increase diuresis, which results in a greater flow of urine into the renal cavities, improving the chances of evacuating the residual fragments of the stone destroyed during flexible ureteroscopy, before they can sediment in the fundus of the renal calices or in the pyelon. Therefore, the investigators hypothesize that a forced diuresis with an injection of Furosemide at the end of ureteroscopy could improve the micro-fragments and stones dust clearance.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Kidney Stone

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Masking Description
    The study will not be blinded except for the outcome assessment: radiologists in charge of interpreting CT-Scans will be blinded.
    Allocation
    Randomized
    Enrollment
    374 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Furosemide
    Arm Type
    Experimental
    Arm Description
    Injection of 40 mg of Furosemide during 10 minutes after the end of the flexible ureteroscopy for destruction of kidney stones with laser.
    Arm Title
    Usual care
    Arm Type
    No Intervention
    Arm Description
    Usual care, without injection of Furosemide.
    Intervention Type
    Drug
    Intervention Name(s)
    Furosemide 40 mg
    Intervention Description
    Injection of 40 mg of Furosemide during 10 minutes after the end of the flexible ureteroscopy for destruction of kidney stones with laser.
    Primary Outcome Measure Information:
    Title
    Rate of stone free patients
    Description
    Rate of stone-free patients 3 months after a flexible ureteroscopy for renal stone laser destruction, evaluated on the low dose abdomino-pelvic CT-Scan. A centralized review of the images will be performed by two specialized radiologists, in a blind and crossed way to allow a homogenization of the results
    Time Frame
    At 3 months
    Secondary Outcome Measure Information:
    Title
    Rate of urinary infection
    Description
    Rate of post-operative urinary tract infection will be assessed within 30 days after surgery on the combination of: Fever higher than 38.5°C and/or, Chills and/or, Clinical symptoms (supra-pubic pain, dysuria, pollakiuria, urgency, urinary burning, back pain radiating to the genitals, hematuria) and/or Positive urine culture with a significant bacteriuria threshold defined as bacteriuria ≥10^5 UFC/mL with one or two bacterial species.
    Time Frame
    From baseline to 30 days
    Title
    Pain in a scale
    Description
    Post-operative pain will be assessed on numerical pain scale in the recovery room, in the service and at the discharge. Pain scale is from 0 (no pain) to 10 (as bad as it could be nothing else matters)
    Time Frame
    During the hospital stay
    Title
    Opioid consumption
    Description
    The use of opioids will be reported
    Time Frame
    During the hospital stay, an average of 1 day
    Title
    Number of participants with adverse events
    Description
    Number of participants with Furosemide adverse events
    Time Frame
    From baseline to 3 months, an average of 1 day

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients ≥ 18 years old and < 80 years old With the need to perform a flexible ureteroscopy with destruction of the kidney stones with laser Participants covered by or entitled to social security Written informed consent obtained from the participant Ability for participant to comply with the requirements of the study Exclusion Criteria: Persons covered by articles L1121-5 to L1121-8 of the CSP (corresponding to all protected persons: pregnant women, parturients, nursing mothers, persons deprived of their liberty by judicial or administrative decision, minors, and persons subject to a legal protection measure: guardianship or trusteeship) Contra-indication to Furosemide: Hyper-sensitivity to the active substance or one of the excipients Hyper-sensitivity to Sulfonamide Renal failure with oligo-anuria refractory to Furosemide Hypokalemia < 3,5 mmol/L Severe hyponatremia Hypovolemia with or without hypotension or dehydration Ongoing hepatitis, hepatic insufficiency severe and hepatic encephalopathy Patient having Furosemide as usual treatment Patient requiring an injection of Aminoside or Vancomycin before or during the procedure Participation in other interventional research with an investigational drug or medical device
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Marie-Lou LETOUCHE, MD
    Phone
    +33247474665
    Email
    marielou.letouche@gmail.com

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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